AESCULAP

Basic Information

• Brand Name: AESCULAP
• Primary DI: 04038653221875
• Version / Model: FF013P
• Catalog Number: FF013P
• Company Name: Aesculap AG
• Labeler DUNS: 315018218
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 200
• Record Status: Published
• Publish Date: 2016-09-23
• Public Version: 4
• Public Version Date: 2020-07-01
• Public Version Status: Update
• Public Device Record Key: eae4962d-f5b0-42eb-abab-0ced5c6314af

Device Description

SCALPFIX STERILE

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: Yes
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
HBO	CLIP, SCALP	Neurology	882.4150	2

GMDN Terms

Code	Name	Definition	Implantable	Status
37458	Scalp haemostasis clip, single-use	A small, manually-operated and applied surgical device used to stop bleeding from the scalp during surgery on the cranium. It is is usually applied to the scalp using the fingers or a dedicated pair of scalp clip forceps, and consists of two blades that are joined at a midpoint. It is typically made of plastic materials. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	04038653221875	GS1
Unit of Use	04038653342679	GS1

Customer Contacts

• Phone: [phone]
• Email: [email protected]